1179360-83-8 Usage
Uses
Used in Organic Chemistry:
1-N-Boc-butane-1,2-diamine-HCl is used as a reagent for the synthesis of various organic compounds, leveraging its ability to introduce protected amine functionalities into target molecules. The Boc protecting group can be selectively removed under acidic conditions, facilitating further reactions or modifications.
Used in Medicinal Chemistry:
In the pharmaceutical industry, 1-N-Boc-butane-1,2-diamine-HCl serves as a key intermediate in the synthesis of a range of pharmaceuticals. Its protected amine groups are crucial for the development of bioactive molecules with specific therapeutic properties. The deprotection of the Boc group allows for the formation of free amines, which can then participate in subsequent reactions to yield the desired drug candidates.
Used in Peptide Synthesis:
1-N-Boc-butane-1,2-diamine-HCl is utilized as a building block in the synthesis of peptides and peptide-based drugs. The Boc protection allows for the stepwise assembly of peptide chains while preventing unwanted side reactions. Once the desired peptide sequence is achieved, the Boc group can be removed to reveal the free amine, enabling further modifications or the formation of peptide bonds.
Used in Catalyst Design:
In catalysis, 1-N-Boc-butane-1,2-diamine-HCl can be employed as a precursor for the development of chiral catalysts. The protected amine groups can be incorporated into catalyst structures, providing opportunities for enantioselective transformations. The subsequent deprotection of the Boc group can lead to the formation of active catalysts with specific selectivity and reactivity.
Used in Material Science:
1-N-Boc-butane-1,2-diamine-HCl can also find applications in the synthesis of functional materials, such as polymers, dendrimers, and self-assembling systems. The protected amine groups can be used to create complex architectures with tailored properties, including stimuli-responsive materials, drug delivery systems, and sensors. The deprotection of the Boc group can be employed to activate or modify the material's properties post-synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 1179360-83-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,9,3,6 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1179360-83:
(9*1)+(8*1)+(7*7)+(6*9)+(5*3)+(4*6)+(3*0)+(2*8)+(1*3)=178
178 % 10 = 8
So 1179360-83-8 is a valid CAS Registry Number.
InChI:InChI=1S/C9H20N2O2.ClH/c1-5-7(10)6-11-8(12)13-9(2,3)4;/h7H,5-6,10H2,1-4H3,(H,11,12);1H
